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The Petasites hybridus CO2 Extract (Ze 339) Blocks SARS-CoV-2 Replication In Vitro.
Urda, Lorena; Kreuter, Matthias Heinrich; Drewe, Jürgen; Boonen, Georg; Butterweck, Veronika; Klimkait, Thomas.
  • Urda L; Department Biomedicine, University of Basel, Petersplatz 10, 4051 Basel, Switzerland.
  • Kreuter MH; Medical Department, Max Zeller & Söhne AG, Seeblickstrasse 4, 8590 Romanshorn, Switzerland.
  • Drewe J; Medical Department, Max Zeller & Söhne AG, Seeblickstrasse 4, 8590 Romanshorn, Switzerland.
  • Boonen G; Medical Department, Max Zeller & Söhne AG, Seeblickstrasse 4, 8590 Romanshorn, Switzerland.
  • Butterweck V; Medical Department, Max Zeller & Söhne AG, Seeblickstrasse 4, 8590 Romanshorn, Switzerland.
  • Klimkait T; Department Biomedicine, University of Basel, Petersplatz 10, 4051 Basel, Switzerland.
Viruses ; 14(1)2022 01 07.
Article in English | MEDLINE | ID: covidwho-1614008
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ABSTRACT
The coronavirus disease 2019 (COVID-19), caused by a novel coronavirus (SARS-CoV-2), has spread worldwide, affecting over 250 million people and resulting in over five million deaths. Antivirals that are effective are still limited. The antiviral activities of the Petasites hybdridus CO2 extract Ze 339 were previously reported. Thus, to assess the anti-SARS-CoV-2 activity of Ze 339 as well as isopetasin and neopetasin as major active compounds, a CPE and plaque reduction assay in Vero E6 cells was used for viral output. Antiviral effects were tested using the original virus (Wuhan) and the Delta variant of SARS-CoV-2. The antiviral drug remdesivir was used as control. Pre-treatment with Ze 339 in SARS-CoV-2-infected Vero E6 cells with either virus variant significantly inhibited virus replication with IC50 values of 0.10 and 0.40 µg/mL, respectively. The IC50 values obtained for isopetasin ranged between 0.37 and 0.88 µM for both virus variants, and that of remdesivir ranged between 1.53 and 2.37 µM. In conclusion, Ze 339 as well as the petasins potently inhibited SARS-CoV-2 replication in vitro of the Wuhan and Delta variants. Since time is of essence in finding effective treatments, clinical studies will have to demonstrate if Ze339 can become a therapeutic option to treat SARS-CoV-2 infections.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Antiviral Agents / Virus Replication / Plant Extracts / SARS-CoV-2 Type of study: Prognostic study Topics: Variants Limits: Animals Language: English Year: 2022 Document Type: Article Affiliation country: V14010106

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Antiviral Agents / Virus Replication / Plant Extracts / SARS-CoV-2 Type of study: Prognostic study Topics: Variants Limits: Animals Language: English Year: 2022 Document Type: Article Affiliation country: V14010106